JPS6112976A - Modification of synthetic fiber - Google Patents

Modification of synthetic fiber

Info

Publication number
JPS6112976A
JPS6112976A JP13362884A JP13362884A JPS6112976A JP S6112976 A JPS6112976 A JP S6112976A JP 13362884 A JP13362884 A JP 13362884A JP 13362884 A JP13362884 A JP 13362884A JP S6112976 A JPS6112976 A JP S6112976A
Authority
JP
Japan
Prior art keywords
fabric
fibers
present
compound
weight
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP13362884A
Other languages
Japanese (ja)
Other versions
JPS6329037B2 (en
Inventor
昌夫 関
菅野 勝男
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Toray Industries Inc
Original Assignee
Toray Industries Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Toray Industries Inc filed Critical Toray Industries Inc
Priority to JP13362884A priority Critical patent/JPS6112976A/en
Publication of JPS6112976A publication Critical patent/JPS6112976A/en
Publication of JPS6329037B2 publication Critical patent/JPS6329037B2/ja
Granted legal-status Critical Current

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  • Chemical Or Physical Treatment Of Fibers (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 (産業上の利用分野ン 本発明はキシミ感と絹鳴りを有し、かつ吸水、制電、S
R性を同時に満足する合IFCIIHの改質方法にWJ
する。
Detailed description of the invention (Industrial field of application)
WJ is a modification method for composite IFCIIH that simultaneously satisfies R properties.
do.

(従来技術) 合IRIl雑は化学的、物理的性質に非常に優れている
が、疎水性繊維であるため、静電気による衣類の身体へ
のまつわりつき、着脱衣時の不快な静電気音の発生、汗
の吸いとりにくさ、洗濯再汚染による黒ずみなどの欠点
を有しており、適用用途が限定されているのが現状であ
る。
(Prior art) IRIl has excellent chemical and physical properties, but since it is a hydrophobic fiber, it causes static electricity to cling to the body, makes unpleasant static noises when putting on and taking off clothes, and causes sweat. It has drawbacks such as difficulty in absorbing water and darkening due to recontamination after washing, and its applications are currently limited.

近年、多性能を有する合成m維の要望が高まり、特公昭
51−2559号でみられるような、重合可能なポリグ
リコール化合物などの親水性化合物で処理し、合成Im
維の表面上に該化合物からなる被膜を形成させて、親水
性能を付与する方iがあるが、この方法ではキシミ感や
絹鳴りなどの特性は発現しない。たとえばポリグリコー
ル化合物の被膜を形成せしめると、大きな風合変化をき
たすと同時に、IIN/繊維、布帛/布帛がすべりやす
くなり、目ズレと称される、布帛構造変化をきたし衣料
用どじての特性を損う問題も生じやすく、キシミ感や絹
鳴りなどの特性も得られない。
In recent years, there has been an increasing demand for synthetic Im fibers with multiple properties, and as seen in Japanese Patent Publication No. 51-2559, synthetic Im fibers are produced by treating them with hydrophilic compounds such as polymerizable polyglycol compounds.
There is a method of imparting hydrophilic properties by forming a film made of the compound on the surface of fibers, but this method does not produce characteristics such as squeaking or silkiness. For example, when a film of a polyglycol compound is formed, it causes a large change in texture, and at the same time, the IIN/fiber and fabric/fabric become slippery, causing a change in the fabric structure called mesh slippage, which is a characteristic for clothing. Problems that impair the quality of the material are likely to occur, and characteristics such as squeaking and silkiness cannot be obtained.

(発明が解決しようとする問題点) 本発明は、キシミ感があり、かつ絹鳴りのする特徴的な
性能を有し、かつ吸水、制電、SR性を同時に満足する
上に、かかる性能が耐久性よく保持される合成繊維を提
供するものである。
(Problems to be Solved by the Invention) The present invention has the characteristic performance of giving a squeaky and silky sound, and satisfies water absorption, antistatic, and SR properties at the same time. The present invention provides synthetic fibers that are retained with good durability.

(問題点を解決するための手段) 無機微粒子を含む分子中に重合可能なビニル基を2個以
上有するポリオキシエヂレングリコール化合物を重合せ
しめて繊維表面に被膜を形成させることを特徴とする合
成繊維の改質方法。
(Means for solving the problem) Synthesis characterized by polymerizing a polyoxyethylene glycol compound having two or more polymerizable vinyl groups in the molecule containing inorganic fine particles to form a film on the fiber surface. Method for modifying fibers.

本発明の無機微粒子を含有するポリオキシエチレングリ
コール化合物を1liI11に付与する方法としては、
浸漬法、パッド・ドライ・キュア法、パッド・スチーム
法、スプレー法、捺染法等があげられるが、パッド・ス
チーム法が、単II雑表面を効率的に被覆しやすいこと
、及び生産性の面力1ら好ましい。すなわち、重合可能
なビニル基を有するポリオキシエチレングリコール化合
物と無機微粒子からなる水溶液に、必要に応じて、重合
開始剤を添加した処理浴に布帛を浸漬した後、マングル
等で絞り、80〜140℃の水蒸気中にて加熱し、重合
反応を開始させ、重合完了後水洗、乾燥するものである
The method for applying the polyoxyethylene glycol compound containing inorganic fine particles of the present invention to 1liI11 is as follows:
Examples include the dipping method, pad dry cure method, pad steam method, spray method, and textile printing method, but the pad steam method has the advantage of being easier to coat III rough surfaces efficiently and in terms of productivity. Force 1 is preferable. That is, after immersing a fabric in a treatment bath containing a polyoxyethylene glycol compound having a polymerizable vinyl group and inorganic fine particles, and adding a polymerization initiator as necessary, the fabric is squeezed with a mangle or the like, and the 80 to 140 The polymerization reaction is initiated by heating in steam at a temperature of 0.degree. C., and after the polymerization is completed, the material is washed with water and dried.

本発明でいう、分子内に重合可能なビニル基を2個以上
有するポリオキシエチレングリコール化合物とは、オキ
シエチレングリコール単位を主構成単位とする親水性化
合物であって、例えばポリエチレングリコールジアクリ
レート、ポリエチレングリコールボリブロビレング植ノ
コールジメタアクリレートポリエチレングリコールω−
(α、′α−ジメタクリロキジメチル)アセテートω′
アクリレートおよび、下記のごときイヒ台物が早番プら
れる。
In the present invention, the polyoxyethylene glycol compound having two or more polymerizable vinyl groups in the molecule is a hydrophilic compound having an oxyethylene glycol unit as a main constituent unit, such as polyethylene glycol diacrylate, polyethylene Glycol polypropylene glycol dimethacrylate polyethylene glycol ω-
(α,′α-dimethacrylokydimethyl)acetate ω′
Acrylate and the following items will be released early.

(但しR1、R2は水素またはメチル基、a−5〜50
0である。) 一般式 (式中R1〜R3はH又は炭素数1〜2のアルキル基。
(However, R1 and R2 are hydrogen or methyl groups, a-5 to 50
It is 0. ) General formula (wherein R1 to R3 are H or an alkyl group having 1 to 2 carbon atoms.

x、y、zは0又は1〜20の整数でx+y+2は3〜
20゜アルキレンエーテル部の一つは必ずエチレンオキ
サイドであることが必要であり、そのモル数は(x +
y +z ) 72以上である。
x, y, z are 0 or integers from 1 to 20, and x+y+2 is from 3 to
One of the 20° alkylene ether moieties must be ethylene oxide, and the number of moles thereof is (x +
y + z) is 72 or more.

Aは一〇−1−NH−1−CH2−1−8O2−1Hs から選ばれた一種の基又は存在しない(ベンゼン核同志
が直接結合する)ことを示す) 本発明でいう無機微粒子とは、酸化アルミニウム、酸化
ケイ素、カオリナイト、タルク、炭酸カルシウム、ケイ
酸カルシウム、酸化マグネシウム、酸化チタン等であり
、粒子径3〜1001μのものをあらかじめ水に分散さ
せておくのが良い。該無機微粒子の中で屈折率の低い例
えば酸化ケイ素などを用いると、被処理布帛の色を濃く
する効果も同時に付与できるものである。
A represents a type of group selected from 10-1-NH-1-CH2-1-8O2-1Hs or does not exist (benzene nuclei are directly bonded to each other). Inorganic fine particles as used in the present invention are: These include aluminum oxide, silicon oxide, kaolinite, talc, calcium carbonate, calcium silicate, magnesium oxide, titanium oxide, etc., and particles with a particle size of 3 to 1001 μm are preferably dispersed in water in advance. If a material having a low refractive index, such as silicon oxide, is used among the inorganic fine particles, the effect of deepening the color of the treated fabric can be imparted at the same time.

該無機微粒子は単独あるいは二種以上混合して使用する
ことができる。使用量は、無機微粒子の種類、粒子径に
より異なるが、使用する親水化化合物1に対し0.05
以上、好ましくは0.1〜0.3である。被処理布帛の
風合に応じて使用量は適宜決定すればよいが、粒子径と
改質効果は、親水化化合物に対し同一重量を混合した場
合、粒子径の小さい方が効果が顕著である。つまり粒子
径の小さいほど、粒子個数が多くなり分布密度が高くな
るためと思われる。また粒子形状は円形状よりも非円形
状のものの方が、キシミ効果が大きい。
The inorganic fine particles can be used alone or in a mixture of two or more. The amount used varies depending on the type and particle size of the inorganic fine particles, but is 0.05 per 1 hydrophilic compound used.
Above, preferably 0.1 to 0.3. The amount used can be determined as appropriate depending on the texture of the fabric to be treated, but the particle size and modification effect are more pronounced when the particle size is smaller when the same weight is mixed with the hydrophilic compound. . In other words, this seems to be because the smaller the particle diameter, the larger the number of particles and the higher the distribution density. Furthermore, the squeaking effect is greater when the particle shape is non-circular than when it is circular.

本発明に用いられる重合開始剤としては、過硫酸アンモ
ニウム、過硫酸カリウム、過酸化水素、過酸化ベンゾイ
ルなどビニル重合開始剤として使ねれる過酸化物および
これらの過酸化物と鉄(II)イオン、亜硫酸塩、ヒド
ロキシルアミンおよびヒドラジンなど還元剤との組合せ
によるレドックス系の開始剤が使われ、かかる重合開始
剤の種類を選択することにより、適宜所望処理条件で処
理することができる。
Polymerization initiators used in the present invention include peroxides that can be used as vinyl polymerization initiators, such as ammonium persulfate, potassium persulfate, hydrogen peroxide, and benzoyl peroxide, and these peroxides and iron (II) ions. A redox initiator in combination with a reducing agent such as sulfite, hydroxylamine, and hydrazine is used, and by selecting the type of polymerization initiator, the treatment can be performed under desired treatment conditions.

本発明は上記ポリオキシエチレングリコール化合物と無
機微粒子を繊維表面に付与することで概ね本発明の目的
は達成されるが、さらに該化合物と無機微粒子の量的な
関係を規制することで、本発明の改善性能を安定して達
成することができる。
In the present invention, the object of the present invention is generally achieved by applying the above-mentioned polyoxyethylene glycol compound and inorganic fine particles to the fiber surface. It is possible to stably achieve improved performance.

該化合物は余り多すぎるとヌメリが強くなり、キシミも
絹鳴りも低下する。たとえば該化合物のみの場合はヌメ
リを抑えるには0.5重量%以下の範囲にその付着量を
規制する必要があるが、これでは吸水性も制電性、SR
性も達成されない。
If the amount of this compound is too large, sliminess becomes strong, and squeaking and silkiness decrease. For example, if only the compound is used, it is necessary to control the amount of adhesion to 0.5% by weight or less in order to suppress slime, but this does not allow for water absorption, antistatic properties, and SR.
Sexuality is also not achieved.

これら全ての性能を安定して付与するには特定な量的隣
保を満足させる。すなわち、該化合物量は雛雑重量に対
して1〜2重量%の範囲に抑え、しかも該無機微粒子の
量は該化合物1部に対して0.05部以上、好ましくは
0.1〜0.3部の範囲に規制するのである。
In order to stably provide all of these performances, certain quantitative conditions must be satisfied. That is, the amount of the compound is suppressed to a range of 1 to 2% by weight based on the weight of the raw material, and the amount of the inorganic fine particles is 0.05 part or more, preferably 0.1 to 0.05 parts, based on 1 part of the compound. It is regulated within the scope of the third section.

本発明の合成繊維とは、通常のポリエステル、ポリアミ
ド、ポリアクリロニトリルなどの合成繊維を意味する。
The synthetic fiber of the present invention means common synthetic fibers such as polyester, polyamide, and polyacrylonitrile.

たとえば、ポリエステル系繊維とはテレフタール酸とエ
チレングリコールあるいはブチレングリコールの縮合反
応によって生成される高分子重合体およびセバシン酸、
アジピン酸、トリメリット酸、イソフタール酸、パラオ
キシ安患香酸などとエチレングリコール、ブチレングリ
コールの縮合重合体ならびに他のポリエステル類たとえ
ば変性ポリエステル、特にカチオン染料可染型ポリエス
テルなどを含むポリエステル系重合体からなる繊維を意
味する。
For example, polyester fibers are polymers produced by the condensation reaction of terephthalic acid and ethylene glycol or butylene glycol, sebacic acid,
Condensation polymers of adipic acid, trimellitic acid, isophthalic acid, paraoxybenzoic acid, etc. with ethylene glycol, butylene glycol, and other polyesters such as modified polyesters, especially polyesters dyeable with cationic dyes, etc. It means the fiber.

また、ポリアミド系繊維とは、ナイロン4.ナイロン6
・6.ナイロン6・10.ナイロン12およびこれらを
変性したナイロン、これらのポリアミド系化合物と他の
高分子体とのブレンド体や共重合体からなる繊維を意味
する。
In addition, polyamide fibers include nylon 4. nylon 6
・6. Nylon 6/10. It refers to fibers made of nylon 12, modified nylons thereof, and blends and copolymers of these polyamide compounds and other polymers.

また、ポリアクリロニトリル系繊維とは、アクリ0ニト
リルを主成分とし、染色性付与を目的に共重合成分とし
て、メチルアクリレート、メチルメタクリレート、スチ
レンスルホン酸ソーダ、アリルスルホン酸ソーダ、2−
メチル−5−ビニルピリジンなどの一種または数種が共
重合された繊維および難燃性を目的に塩化ビニリデンな
どが共重合またはブレンドされた繊維を言う。
In addition, polyacrylonitrile fibers are mainly composed of acrylonitrile, and are copolymerized with methyl acrylate, methyl methacrylate, sodium styrene sulfonate, sodium allyl sulfonate, 2-
It refers to fibers copolymerized with one or more types of methyl-5-vinylpyridine, and fibers copolymerized or blended with vinylidene chloride for the purpose of flame retardancy.

なお、合成繊維のうちでも、ポリエステル系繊維、特に
異形断面糸、なかでも絹様外観を有する高級衣料用at
雑に本発明は極めて効果的である。
Among synthetic fibers, polyester fibers, especially irregular cross-section yarns, and especially AT for high-grade clothing having a silk-like appearance.
Overall, the present invention is extremely effective.

すなわち、かかる繊維に本発明でいう多性能ならびにキ
シミ感、絹鳴り特性を付与したものは、強伸度の点から
天然の絹にも優る衣料用材料となる。
In other words, such fibers imparted with the multi-performance as well as squeaky and silky characteristics as defined in the present invention become materials for clothing that are superior to natural silk in terms of strength and elongation.

その中でも異形断面であって、かつ第1図のように凸部
に溝を有する繊維の場合はその繊維に特有なキシミ感や
絹鳴り等を損わないので、本発明法が特に好都合である
。かかるlll1tは、たとえば凸。
Among these, the method of the present invention is particularly advantageous in the case of fibers with irregular cross-sections and grooves in the convex portions as shown in Fig. 1, since it does not impair the squeakiness or silkiness characteristic of the fibers. . Such lll1t is, for example, convex.

部に易溶出成分を配置し、複合紡糸して、アルカ。Place the easily eluting components in the parts, composite spin, and alkali.

り処理を施すことによって容易に製造できる。It can be easily manufactured by subjecting it to a similar treatment.

また、合成Il#は単独でも混用されていても、その形
態が糸または布帛になった形態でもステープル状態にな
っていてもさしつかえないが、それらの形態のうちでも
、布帛形態が特に効果が発揮される。
In addition, synthetic Il# may be used alone or in combination, and may be in the form of thread or fabric, or in the form of staples, but among these forms, the fabric form is particularly effective. be done.

(実施例) 実施例1 50デニール36フイラメントからなる三角断面を有す
るポリエステル糸(東しく株)製)に250T/Mの撚
をほどこしたものをタテ糸に、75デニール36フイラ
メントの三角断面糸(東しく株)製)を仮ヨリ加工後1
200T/Mの追撚したものを緯糸に用い、サテンクレ
ープを製織した。
(Example) Example 1 A polyester yarn (manufactured by Toshiku Co., Ltd.) having a triangular cross section made of 50 denier 36 filaments and twisted at 250 T/M was used as a warp yarn, and a triangular cross section yarn (75 denier 36 filament) was used as a warp yarn. (manufactured by Toshiku Co., Ltd.) after temporary twisting 1
A satin crepe was woven using 200 T/M additional twist as the weft.

次いで常法によりワッシャーでシボ立加工し、180℃
のI!度でヒートセットを施し、50g/ffiのカセ
イソーダ−を含む98℃の水溶液中でアルカリ減量し、
中和、水洗した後、160℃の温度で仕上セットした。
Next, it is embossed using a washer using a conventional method, and heated to 180°C.
I! heat-set at 30°C, alkali weight loss was performed in a 98°C aqueous solution containing 50g/ffi of caustic soda,
After neutralization and washing with water, final setting was carried out at a temperature of 160°C.

アルカリ減量率は20%であり、得られた布帛は、絹様
のふくらみ、ドレープ性をもつ優れたものである。
The alkali weight loss rate was 20%, and the fabric obtained had excellent silk-like fluff and drape properties.

該織物を下記処理浴に浸漬後マングルで均一に絞って付
@量を90重@%に調整した。次いで130℃の加熱水
蒸気中にて5分間処理し、しかる後、潮洗(60℃)、
水洗した後乾燥し160℃の温度で、ヒートセットした
The fabric was immersed in the treatment bath described below and then squeezed uniformly with a mangle to adjust the weight to 90% by weight. Next, it was treated in heated steam at 130°C for 5 minutes, and then washed (60°C).
After washing with water, it was dried and heat set at a temperature of 160°C.

処理浴は、ポリオキシエチレンセグメントの分子量が1
000であるポリエチレングリコールジメタアクリレー
ト30g/Qの水溶液に重合開始剤として過硫酸アンモ
ニウム3g/ρ添加したものに、40〜50mμの粒子
径をもつ酸化ケイ素をあらかじめ20重量%の濃度で水
中に分散させたものを10.20、sog/Q添加した
。比較例1として酸化ケイ素を含まない処理浴を使用し
た比較例2として比較例1で処理した織物を本発明法の
酸化ケイ素水分散液20g / Qの処理浴に浸漬し9
0重量%の付着になるようマングルで絞った後160℃
の温度でキユアリングした。
In the treatment bath, the molecular weight of the polyoxyethylene segment is 1.
To an aqueous solution of 30 g/Q of polyethylene glycol dimethacrylate (000) and 3 g/ρ of ammonium persulfate as a polymerization initiator, silicon oxide having a particle size of 40 to 50 mμ was preliminarily dispersed in water at a concentration of 20% by weight. 10.20 sog/Q was added. As Comparative Example 1, a treatment bath not containing silicon oxide was used.As Comparative Example 2, the fabric treated in Comparative Example 1 was immersed in a treatment bath containing 20 g/Q of the silicon oxide aqueous dispersion of the present invention.
160℃ after squeezing with a mangle so that the adhesion is 0% by weight.
cured at a temperature of

耐洗濯性を見るため、処理布の一部を2g/Qの中性洗
剤(ザブ、花王石鹸製)水溶液中で40℃で5分間洗濯
を繰返し10回実施した。洗濯前後の処理布について、
親水性性能評価として、樹脂付着率、吸水性、制電性、
ヌメリ属台特性として静摩擦力、目ズレ特性として織物
の緯糸の引き抜き抵抗値を測定し、これらの測定結果を
表1に示した。
To examine washing resistance, a portion of the treated fabric was washed 10 times at 40° C. for 5 minutes in a 2 g/Q aqueous solution of a neutral detergent (ZABU, manufactured by Kao Soap). Regarding treated fabric before and after washing,
As hydrophilic performance evaluation, resin adhesion rate, water absorption, antistatic property,
Static friction force was measured as the slime property, and pull-out resistance of the weft yarn of the fabric was measured as the slippage property, and the results of these measurements are shown in Table 1.

なお、性能評価寸法は次の通りである。The dimensions for performance evaluation are as follows.

樹脂付着率:処理前後の重量変化より求めた。Resin adhesion rate: Determined from the weight change before and after treatment.

吸 水 性:処理布上に一滴が約0.03m1の水滴を
落とし、それが完全に吸収される までの時間を測定した。
Water absorption: A water droplet of approximately 0.03 ml was dropped onto the treated cloth, and the time until it was completely absorbed was measured.

制電性(摩擦帯電圧):京大化研式0−タリースタチッ
クテスターを用い、綿布を対 象布として20℃、30%RHの雰囲気中での摩擦帯電
圧(V)を測定した。
Antistatic property (frictional charging voltage): Frictional charging voltage (V) was measured in an atmosphere of 20° C. and 30% RH using a cotton cloth as a target cloth using a Kyoto University Kaken type 0-tally static tester.

静摩擦カニ[繊維と工業J vol 31.へ10 (
1975)PI3にあるような装置を組み立てス ティック−スリップ曲線を求め、曲 線から静摩擦力(9)を測定した。
Static friction crab [Textile and Industry J vol 31. to 10 (
A stick-slip curve was obtained by assembling a device similar to PI3 (1975), and the static friction force (9) was measured from the curve.

目ズレ抵抗度: J I S L1096B法に基づき
緯糸の引き抜き抵抗値(9)を求めた。
Weft resistance: Weft pull-out resistance (9) was determined based on the JIS L1096B method.

表1から本発明によるものは親水性化合物の性能を損う
ことなく比較例1にみられる静摩擦力低下による風合の
ヌメリ、目ズレ抵抗度低下による品質低下がおさえられ
、未加工品と同等の風合、品質を維持できるのが判る。
From Table 1, the product according to the present invention suppresses the slippage of the texture due to the decrease in static friction force and the quality deterioration due to the decrease in the resistance to shedding seen in Comparative Example 1 without impairing the performance of the hydrophilic compound, and is equivalent to the unprocessed product. It is clear that the texture and quality can be maintained.

本発明の中でも酸化ケイ素20Q/Q添加のものが、最
も未加工に近い風合であった。なお比較例2は、洗濯0
回では未加工品の風合特性に近いものが得られるが、洗
濯による耐久性がなく実用性に乏しい。
Among the products according to the present invention, the one containing 20Q/Q silicon oxide had the texture closest to that of an unprocessed product. In addition, in Comparative Example 2, no washing was performed.
Although it is possible to obtain a texture similar to that of an unprocessed product, it is not durable against washing and is of little practical use.

実施例2 易溶解性ポリマとしてポリエチレンテレフタレート(固
有粘度0.66 、酸化チタン0.55%含有)とポリ
エチレンテレフタレート(98モル%)15−ソジュー
ムスルホイソフタレート(2モル%)とからなる共重合
ポリエステル(25℃オルトクロロフェノール中の固有
粘度0.55 )の重量比80/20の混合物、難溶解
性ポリマとして上記ポリエチレンテレフタレートを用い
紡糸温度295℃、紡糸速度1200■/sin 、易
溶解性ポリマ:難溶解性ポリマを20:80として易溶
解性ポリマをY型吐出孔の各先端部に芯鞘状に供給して
複合紡糸し、引続き延伸速度3001+1/Sin 、
熱ピン温度120℃、延伸倍率3.3倍で延伸し、三ケ
所の頂点に易溶解性ポリマを含む三角断面形状を有する
75デニール36フイラメントの延伸糸とした。易溶解
性ポリマの繊維表面に占める長さは160μであり、易
溶解性ポリマの中で繊維重心にもっとも近い点と遠い点
の間の長さは2.5μであった。なお易溶解性ポリマの
難溶解性ポリマに対する溶解速度比は後で述べる溶解処
理条件下で4倍である。
Example 2 Copolymerization of easily soluble polymers consisting of polyethylene terephthalate (intrinsic viscosity 0.66, titanium oxide content 0.55%), polyethylene terephthalate (98 mol%) and 15-sodium sulfoisophthalate (2 mol%) A mixture of polyester (intrinsic viscosity 0.55 in orthochlorophenol at 25°C) in a weight ratio of 80/20, using the above polyethylene terephthalate as the poorly soluble polymer, spinning temperature 295°C, spinning speed 1200 cm/sin, easily soluble polymer. : A slightly soluble polymer was mixed with a ratio of 20:8, and a easily soluble polymer was supplied in a core-sheath shape to each tip of the Y-shaped discharge hole for composite spinning, followed by a drawing speed of 3001+1/Sin.
The yarn was drawn at a hot pin temperature of 120° C. and a draw ratio of 3.3 times to obtain a drawn yarn of 75 denier 36 filament having a triangular cross-sectional shape containing easily soluble polymer at three vertices. The length of the easily soluble polymer on the fiber surface was 160 μm, and the length between the point closest to the fiber center of gravity and the point farthest from the center of gravity of the easily soluble polymer was 2.5 μm. Note that the dissolution rate ratio of the easily soluble polymer to the slightly soluble polymer is 4 times that of the slightly soluble polymer under the dissolution treatment conditions described later.

この延伸糸を用いて、経糸には150T / Mの撚を
施し緯糸として900T/MのS方向で撚りをかけたも
のを2本引き揃えた後700T/Mの7方向の撚を施し
た駒撚り糸を用い、ジャガード織機で和装用の駒椴子を
製織した。得られた織物を精練後180℃の温度で中間
セット、30g/aのカセイソーダ水溶液により100
℃でアルカリ処理して頂点に入口幅1.2μ深さ1.9
μの溝を有する三角断面糸を形成せしめた。
Using this drawn yarn, the warp was twisted at 150T/M, and the weft was twisted at 900T/M in the S direction, then two yarns were pulled together and then twisted at 700T/M in 7 directions to create a piece. Using twisted thread, we wove komazu for Japanese clothing on a jacquard loom. After scouring the obtained fabric, it was heated to 180°C for an intermediate setting and heated to 100°C with a 30g/a caustic soda aqueous solution.
Inlet width 1.2μ depth 1.9 at the apex after alkali treatment at ℃
A triangular cross-section thread with μ grooves was formed.

次いで0ianix 31ack  BG−FS (三
ll化成(株)製分散染料)14%owfを含む浴比1
対30の染色浴中で130℃で60分間染色した後、常
法に従い還元洗浄を行ない、水洗、乾燥した。
Next, 0ianix 31ack BG-FS (disperse dye manufactured by Sanll Kasei Co., Ltd.) was added to a bath containing 14% owf at a bath ratio of 1.
After dyeing at 130° C. for 60 minutes in a 30% dye bath, reduction cleaning was performed according to a conventional method, followed by washing with water and drying.

この黒色染色物を次の処理浴に浸漬後、マングルで均一
に絞り付@量を80重量%に調整し、次いで105℃の
飽和水蒸気中で3分間処理し凋洗(60℃)、水洗した
後170℃のwA痕でヒートセットして第1図のlN雑
を得た。
This black dyed product was immersed in the following treatment bath, then squeezed uniformly with a mangle to adjust the amount to 80% by weight, then treated in saturated steam at 105°C for 3 minutes, washed (60°C), and washed with water. After that, it was heat set at 170° C. to obtain the 1N roughness shown in FIG.

本発明の処理浴:ポリオキシエチレンセグメントの分子
量が2000であるポリエチレングリコールトリメタク
リレート25g/Qの水溶液に重合開始剤として過硫酸
アンモニウム29/a添加し粒子径が10〜29.mμ
の酸化ケイ素を20重量%の濃度であらかじめ水中に均
一に分散させたものを25g/Q添加。
Treatment bath of the present invention: Ammonium persulfate 29/a as a polymerization initiator is added to an aqueous solution of 25 g/Q of polyethylene glycol trimethacrylate whose polyoxyethylene segment has a molecular weight of 2000, and the particle size is 10 to 29. mμ
Add 25g/Q of silicon oxide uniformly dispersed in water at a concentration of 20% by weight.

比較例の処理浴:上記ポリエチレングリコールトリメタ
クリレートと過硫酸アンモニウムのみからなるもの。
Treatment bath of comparative example: one consisting only of the above polyethylene glycol trimethacrylate and ammonium persulfate.

実施例1と同様に測定した親水性性能、風合物性の結果
を表2に示した。
Table 2 shows the results of hydrophilicity performance and texture and physical properties measured in the same manner as in Example 1.

ここでスティックスリップとは静11!II力測定時の
スティック−スリップ曲線の振幅から求めた値で布帛の
キシミ感を示すもので大きい値はどキシミ感のある風合
である。またL値とは色の濃さを示すもので、デジタル
測色色差計(スガ試験機(株)製)で測定したもので、
L値の小さいほど視感濃度が濃いことを表わす。
Here, stick-slip is Shizuka 11! II The value obtained from the amplitude of the stick-slip curve during force measurement indicates the squeaky feel of the fabric, and a large value indicates a squeaky texture. In addition, the L value indicates the depth of color, and is measured with a digital colorimeter (manufactured by Suga Test Instruments Co., Ltd.).
The smaller the L value, the higher the visual density.

本発明によれば、キシミ感を有する高級シルキー素材の
特長を損うことのない耐久性に優れた親水化処理物を得
ることができ、被染物の色を濃くする効果も同時に得る
ことができる。
According to the present invention, it is possible to obtain a hydrophilized product with excellent durability that does not impair the characteristics of the high-grade silky material that has a squeaky feel, and it is also possible to obtain the effect of deepening the color of the dyed object at the same time. .

(発明の効果) 本発明は、キシミ感があり、かつ絹鳴りのする特徴的な
性能に加えて吸水、訓電、SR性を同時に満足し、しか
もかかる性能が耐久性よく保持される合成繊維を提供す
るものである。
(Effects of the Invention) The present invention provides a synthetic fiber that satisfies water absorption, electric shock, and SR properties at the same time in addition to the characteristic performance of squeaking and silky sound, and also maintains these properties with good durability. It provides:

本発明によって改質された合成繊維は画板衣料、特に和
装用途に好適な材料である。
The synthetic fibers modified according to the present invention are suitable materials for drawing board clothing, especially for Japanese clothing.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は本発明方法に係る繊維の代表的なものの断面を
示す模式図である。 図中 1:繊維 2:ポリオキシエチレングリコール化合物被膜層3:無
機微粒子 特許出願人  東 し 株 式 会 社第11
FIG. 1 is a schematic diagram showing a cross section of a typical fiber according to the method of the present invention. In the figure 1: Fiber 2: Polyoxyethylene glycol compound coating layer 3: Inorganic fine particles Patent applicant Toshi Co., Ltd. Company No. 11

Claims (1)

【特許請求の範囲】[Claims] 無機微粒子を含む分子中に重合可能なビニル基を2個以
上有するポリオキシエチレングリコール化合物を重合せ
しめて繊維表面に被膜を形成させることを特徴とする合
成繊維の改質方法。
A method for modifying synthetic fibers, which comprises polymerizing a polyoxyethylene glycol compound having two or more polymerizable vinyl groups in a molecule containing inorganic fine particles to form a film on the fiber surface.
JP13362884A 1984-06-28 1984-06-28 Modification of synthetic fiber Granted JPS6112976A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13362884A JPS6112976A (en) 1984-06-28 1984-06-28 Modification of synthetic fiber

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13362884A JPS6112976A (en) 1984-06-28 1984-06-28 Modification of synthetic fiber

Publications (2)

Publication Number Publication Date
JPS6112976A true JPS6112976A (en) 1986-01-21
JPS6329037B2 JPS6329037B2 (en) 1988-06-10

Family

ID=15109259

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13362884A Granted JPS6112976A (en) 1984-06-28 1984-06-28 Modification of synthetic fiber

Country Status (1)

Country Link
JP (1) JPS6112976A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4832276A (en) * 1988-04-18 1989-05-23 Usx Corporation Polyurethane sleeve for tension reels
JP2007070744A (en) * 2005-09-05 2007-03-22 Toray Ind Inc Textile fiber structural product
JP2016084548A (en) * 2014-10-23 2016-05-19 帝人株式会社 Fabric, fiber product and method of treating fabric

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6092560B2 (en) * 2012-09-28 2017-03-08 ユニチカトレーディング株式会社 Dust-free garment and method for producing the same

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5119898A (en) * 1974-08-07 1976-02-17 Mitsubishi Rayon Co GOSEISENIYOSHIN SUIKASHORIZAI
JPS5766184A (en) * 1980-10-08 1982-04-22 Toray Industries Fiber structure treated by resin and production thereof

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5119898A (en) * 1974-08-07 1976-02-17 Mitsubishi Rayon Co GOSEISENIYOSHIN SUIKASHORIZAI
JPS5766184A (en) * 1980-10-08 1982-04-22 Toray Industries Fiber structure treated by resin and production thereof

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4832276A (en) * 1988-04-18 1989-05-23 Usx Corporation Polyurethane sleeve for tension reels
JP2007070744A (en) * 2005-09-05 2007-03-22 Toray Ind Inc Textile fiber structural product
JP2016084548A (en) * 2014-10-23 2016-05-19 帝人株式会社 Fabric, fiber product and method of treating fabric

Also Published As

Publication number Publication date
JPS6329037B2 (en) 1988-06-10

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